Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3640243018 | Autosomal dominant spastic paraplegia type 37 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3640244012 | Autosomal dominant spastic paraplegia type 37 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3640245013 | A pure form of hereditary spastic paraplegia with a childhood to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense at ankles and urinary dysfunction. Ankle clonus is also reported in some patients. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant spastic paraplegia type 37 | Associated morphology | Degenerative abnormality | false | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 37 | Is a | Autosomal dominant hereditary spastic paraplegia | true | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 37 | Clinical course | Progressive | true | Inferred relationship | Some | 3 | |
| Autosomal dominant spastic paraplegia type 37 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 37 | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 37 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 37 | Interprets | Movement | true | Inferred relationship | Some | 6 | |
| Autosomal dominant spastic paraplegia type 37 | Finding site | Structure of right lower limb | true | Inferred relationship | Some | 4 | |
| Autosomal dominant spastic paraplegia type 37 | Finding site | Structure of left lower limb | true | Inferred relationship | Some | 5 | |
| Autosomal dominant spastic paraplegia type 37 | Interprets | Movement observable | true | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 37 | Has interpretation | Absent | true | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 37 | Is a | Autosomal dominant hereditary disorder | false | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 37 | Is a | Pure hereditary spastic paraplegia | true | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 37 | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 37 | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 37 | Finding site | Structure of lower limb | false | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 37 | Associated morphology | Degeneration | false | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 37 | Finding site | Spinal cord structure | false | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR